Dimethyl carbonate for environmentally benign reactions

被引:148
作者
Ono, Y
机构
[1] Department of Chemical Engineering, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo
关键词
D O I
10.1351/pac199668020367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dimethyl carbonate (DMC) is a unique molecule having a versatile reactivity, The transesterification of DMC with phenol gives methyl phenyl carbonate, which is converted into diphenyl carbonate (DPC) by the disproportionation. MoO3/SiO2 is an active catalyst for both reactions. DPC is an essential monomer in the non-phosgene route for polycarbonates. The methoxycarbonylation of aniline gives methyl N-phenyl carbamate in the presence of a lead compound. This reaction offers a non-phosgene route to isocyanates. As a methylating agent, DMC can be a substitute for methyl halides and dimethyl sulfate, toxic and corrosive chemicals. Phenylacetylene, aniline and phenol are selectively methylated with DMC over zeolites in the vapor-phase. The reaction of DMC with silica offers a simple and clean method for synthesizing Si(OCH3)(4).
引用
收藏
页码:367 / 375
页数:9
相关论文
共 46 条
  • [1] DIRECT SYNTHESIS OF TETRAMETHOXYSILANE FROM RICE HULL ASH BY REACTION WITH DIMETHYL CARBONATE
    AKIYAMA, M
    SUZUKI, E
    ONO, Y
    [J]. INORGANICA CHIMICA ACTA, 1993, 207 (02) : 259 - 261
  • [2] AN EXCEPTIONALLY MILD, CATALYTIC HOMOGENEOUS METHOD FOR THE CONVERSION OF AMINES INTO CARBAMATE ESTERS
    ALPER, H
    HARTSTOCK, FW
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (16) : 1141 - 1142
  • [3] CONVERSION OF PRIMARY AMINES TO CARBAMATE ESTERS USING PALLADIUM-CHLORIDE AND DI-TERT-BUTYL PEROXIDE - DOUBLE CARBONYLATION OF SECONDARY-AMINES
    ALPER, H
    VASAPOLLO, G
    HARTSTOCK, FW
    MLEKUZ, M
    SMITH, DJH
    MORRIS, GE
    [J]. ORGANOMETALLICS, 1987, 6 (11) : 2391 - 2393
  • [4] AWATO I, 1993, SCIENCE, V259, P1538
  • [5] THE "BIS(SALICYLALDEHYDE)ETHYLENEDIIMINE COBALT(II)-CATALYZED OXIDATIVE CARBONYLATION OF PRIMARY AND SECONDARY-AMINES
    BENEDINI, F
    NALI, M
    RINDONE, B
    TOLLARI, S
    CENINI, S
    LAMONICA, G
    PORTA, F
    [J]. JOURNAL OF MOLECULAR CATALYSIS, 1986, 34 (02): : 155 - 161
  • [6] SELECTIVE RUTHENIUM CARBONYL CATALYZED REDUCTIVE CARBONYLATION OF AROMATIC NITRO-COMPOUNDS TO CARBAMATES
    CENINI, S
    PIZZOTTI, M
    CROTTI, C
    PORTA, F
    LAMONICA, G
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1984, (19) : 1286 - 1287
  • [7] CENTI S, 1988, J ORG CHEM, V53, P1243
  • [8] CUSUMANO JA, 1992, CHEMTECH, P482
  • [9] FROST JW, 1995, CHEM BRIT, V3, P207
  • [10] Fu Z., UNPUB